Answers are grounded in this paper and cite their sources.
A common-intermediate-based enantioselective strategy has been developed aiming at bicyclic arene cis-dihydrodiols, cis-4-hydroxyscytalones, and bicyclic mimics of conduritol. Key features of this protocol include Barrett's asymmetric hydroxyallylation, ring-closing metathesis (RCM), and completely regioselective Wacker oxidation of internal cyclic olefins.
No takes yet. Share an insight, caveat, or question.
Mukherjee et al. (2010) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: